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Abbott Nutrition, Division of Abbott Laboratories Recall: a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.

United States

TerminatedClass II

Company
Abbott Nutrition, Division of Abbott Laboratories
Product
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 p…
Recall date
August 16, 2019
Terminated
December 4, 2019
Source
FDA

Reason for recall

a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton. Not published in this source record 13440 cartons but only 550 cartons (6600 bottles) affected Carton Batch # 06108XK00; Bottle Batch # 02567X800

Distribution

  • Distribution Centers in: Alabama
  • Iowa
  • Minneapolis
  • North Carolina
  • New York
  • Ohio
  • South Carolina
  • Virginia
  • Wisconsin

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-2153-2019
Event ID
83608
Status
Terminated
Classification
Class II
Company
Abbott Nutrition, Division of Abbott Laboratories
Product description
Similac Pro-Sensitive, 2 fl. oz. plastic bottles packed 12 per carton.
Quantity
13440 cartons but only 550 cartons (6600 bottles) affected
Reason
a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.
Recall initiation date
August 16, 2019
Report date
September 18, 2019
Classification date
Not published in this source record
Termination date
December 4, 2019
Distribution pattern
Distribution Centers in: Alabama, Iowa, Minneapolis, North Carolina, New York, Ohio, South Carolina, Virginia, Wisconsin
UPC, lot, and code information
Carton Batch # 06108XK00; Bottle Batch # 02567X800
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Abbott Nutrition, Division of Abbott Laboratories

Other recalls from Abbott Nutrition, Division of Abbott Laboratories

FDA Recall United States Terminated Historical recordClass III

Abbott Nutrition, Division of Abbott Laboratories

Product
Similac Pro-Advance Infant Formula with Iron, Milk-Based, Re…
Published
July 22, 2020
Distribution
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Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

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